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Biomechanical force may promote tumor progression by establishing an aggressive tumor cell hierarchy. Biomechanical force may promote tumor progression.

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Presentation on theme: "Biomechanical force may promote tumor progression by establishing an aggressive tumor cell hierarchy. Biomechanical force may promote tumor progression."— Presentation transcript:

1 Biomechanical force may promote tumor progression by establishing an aggressive tumor cell hierarchy. Biomechanical force may promote tumor progression by establishing an aggressive tumor cell hierarchy. In a hierarchical model of tumorigenesis, transformation may originate from among any of the different lineages that form a tissue including stem cells, progenitor cells, or their differentiated progeny. Normal stem and progenitor cells are intrinsically programmed for self-renewal and survival; therefore, their dysregulation could generate CSCs or tumor-initiating cells (TIC) with similar capacities for self-renewal and the propagation of differentiated tumor cells. Alternatively, CSCs may be derived from oncogenic events occurring in mature somatic cells that enable the acquisition of CSC properties. Alterations to biomechanical forces through a transformed physical and genetic landscape may contribute to CSC formation by favoring the proliferative expansion of a specific stem/progenitor population, or by inducing an EMT and the dedifferentiation of more differentiated transformed cells. An expanded progenitor population represents an attractive long-lived target for the accumulation of oncogenic mutations and tumor initiation. A stochastic model of tumor progression suggests the stepwise acquisition of sporadic mutations and clonal evolution through competitive selection. In all likelihood, tumors develop through mechanisms that include both hierarchical and stochastic models, and force-induced tissue remodeling and programming of tumor cells may play a significant role in regulating tumor heterogeneity and tumor cell plasticity. Jason J. Northey et al. Cancer Discov 2017;7: ©2017 by American Association for Cancer Research


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